UB Paderborn / Katalog / Suche / in CDI

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 1997-11, Vol.399 (2), p.382-390

1997

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Therapeutic Potential of N-Acetyl-Glucagon-Like Peptide-1 in Primary Motor Neuron Cultures Derived From Non-Transgenic and SOD1-G93A ALS Mice

Cellular and molecular neurobiology, 2013-04, Vol.33 (3), p.347-357

2013

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Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group

Journal of neurology, 2020-07, Vol.267 (7), p.2130-2141

2020

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Nerve ultrasound findings in Sjögren's syndrome‐associated neuropathy

Journal of neuroimaging, 2021-11, Vol.31 (6), p.1156-1165

2021

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Percutaneous endoscopic gastrostomy with and without jejunal extension in patients with amyotrophic lateral sclerosis

European journal of gastroenterology & hepatology, 2018-03, Vol.30 (3), p.257-262

2018

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Altered expression of DJ-1 and PINK1 in sporadic ALS and in the SOD1(G93A) ALS mouse model

Journal of neuropathology and experimental neurology, 2013-11, Vol.72 (11), p.1052-1061

2013

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Nrf2/ARE Signaling Pathway: Key Mediator in Oxidative Stress and Potential Therapeutic Target in ALS

Neuro-Sjögren: Peripheral Neuropathy With Limb Weakness in Sjögren's Syndrome

Clinical characterisation of women with persistent genital arousal disorder: the iPGAD-study

Onset and spreading patterns of upper and lower motor neuron symptoms in amyotrophic lateral sclerosis

Analysis of routine blood parameters in patients with amyotrophic lateral sclerosis and evaluation of a possible correlation with disease progression—a multicenter study

Peripheral nerve atrophy together with higher cerebrospinal fluid progranulin indicate axonal damage in amyotrophic lateral sclerosis

Neurological management and work-up of neurotoxicity associated with CAR T cell therapy

Anti-ganglioside antibodies in amyotrophic lateral sclerosis revisited

Weight loss, dysphagia and supplement intake in patients with amyotrophic lateral sclerosis (ALS): impact on quality of life and therapeutic options

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis

Validation of the German version of the extended ALS functional rating scale as a patient-reported outcome measure

The Axon Guidance Protein Semaphorin 3A Is Increased in the Motor Cortex of Patients With Amyotrophic Lateral Sclerosis

Widespread grey matter pathology dominates the longitudinal cerebral MRI and clinical landscape of amyotrophic lateral sclerosis

Expression of the axon‐guidance protein receptor Neuropilin 1 is increased in the spinal cord and decreased in muscle of a mouse model of amyotrophic lateral sclerosis

Decreased mRNA Expression of PGC-1α and PGC-1α–Regulated Factors in the SOD1G93A ALS Mouse Model and in Human Sporadic ALS

Interaction of physical function, quality of life and depression in Amyotrophic lateral sclerosis: characterization of a large patient cohort

Cranial nerve involvement in patients with immune-mediated neuropathy: An observational blink reflex study

Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy

CIDP associated with Sjögren’s syndrome

Design of a new CCD-camera neutron radiography detector

Therapeutic Potential of N-Acetyl-Glucagon-Like Peptide-1 in Primary Motor Neuron Cultures Derived From Non-Transgenic and SOD1-G93A ALS Mice

Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group

Nerve ultrasound findings in Sjögren's syndrome‐associated neuropathy

Percutaneous endoscopic gastrostomy with and without jejunal extension in patients with amyotrophic lateral sclerosis

Altered expression of DJ-1 and PINK1 in sporadic ALS and in the SOD1(G93A) ALS mouse model

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